Loading…
Access to New Reactive Unsaturated Cycloalkenethiones by Flash Vacuum Thermolysis
The reactive conjugated cycloalkenethiones (3, 4, 5) have been synthesized from the corresponding cycloalkenylsulfanyl compounds under flash vacuum thermolysis (FVT) conditions. The nonconjugated cycloalkenethiones (8, 9) were prepared in the same way, the tautomerisation into cycloalkadienethiols (...
Saved in:
Published in: | Phosphorus, sulfur, and silicon and the related elements sulfur, and silicon and the related elements, 1999-01, Vol.153 (1), p.387-388 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c296t-7a4cd69994877ac476164231b803171812b1d0e1b086333a5685d550daf39ecc3 |
container_end_page | 388 |
container_issue | 1 |
container_start_page | 387 |
container_title | Phosphorus, sulfur, and silicon and the related elements |
container_volume | 153 |
creator | Briard, Emmanuelle Levillain, Jocelyne Ripoll, Jean-Louis |
description | The reactive conjugated cycloalkenethiones (3, 4, 5) have been synthesized from the corresponding cycloalkenylsulfanyl compounds under flash vacuum thermolysis (FVT) conditions. The nonconjugated cycloalkenethiones (8, 9) were prepared in the same way, the tautomerisation into cycloalkadienethiols (10, 11) occurred at 77 K. As for the cyclobutenethione 13, only the ring opening products were observed at 77 K. |
doi_str_mv | 10.1080/10426509908546484 |
format | article |
fullrecord | <record><control><sourceid>crossref_infor</sourceid><recordid>TN_cdi_crossref_primary_10_1080_10426509908546484</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_10426509908546484</sourcerecordid><originalsourceid>FETCH-LOGICAL-c296t-7a4cd69994877ac476164231b803171812b1d0e1b086333a5685d550daf39ecc3</originalsourceid><addsrcrecordid>eNqF0M1Kw0AQB_BFFKzVB_C2LxDdzX6Dl1KsCkVRWq9hstnQaJKV3a01b2-k3op4moGZ3wz8Ebqk5IoSTa4p4bkUxBiiBZdc8yM0oUKyTLBcHI_9OM_GBXWKzmJ8I4SYnJEJep5Z62LEyeNHt8MvDmxqPh1e9xHSNkByFZ4PtvXQvrvepU3jexdxOeBFC3GDX8Futx1ebVzofDvEJp6jkxra6C5-6xStF7er-X22fLp7mM-Wmc2NTJkCbitpjOFaKbBcSSp5zmipCaOKapqXtCKOlkRLxhgIqUUlBKmgZsZZy6aI7u_a4GMMri4-QtNBGApKip9MioNMRqP2pulrHzrY-dBWRYKh9aEO0NsmHqoifaVR3vwr2d-PvwEnF3kb</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Access to New Reactive Unsaturated Cycloalkenethiones by Flash Vacuum Thermolysis</title><source>Taylor and Francis Science and Technology Collection</source><creator>Briard, Emmanuelle ; Levillain, Jocelyne ; Ripoll, Jean-Louis</creator><creatorcontrib>Briard, Emmanuelle ; Levillain, Jocelyne ; Ripoll, Jean-Louis</creatorcontrib><description>The reactive conjugated cycloalkenethiones (3, 4, 5) have been synthesized from the corresponding cycloalkenylsulfanyl compounds under flash vacuum thermolysis (FVT) conditions. The nonconjugated cycloalkenethiones (8, 9) were prepared in the same way, the tautomerisation into cycloalkadienethiols (10, 11) occurred at 77 K. As for the cyclobutenethione 13, only the ring opening products were observed at 77 K.</description><identifier>ISSN: 1042-6507</identifier><identifier>EISSN: 1563-5325</identifier><identifier>DOI: 10.1080/10426509908546484</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>cycloalkenethione ; flash vacuum thermolysis ; retro-ene ; vinylthioketene</subject><ispartof>Phosphorus, sulfur, and silicon and the related elements, 1999-01, Vol.153 (1), p.387-388</ispartof><rights>Copyright Taylor & Francis Group, LLC 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c296t-7a4cd69994877ac476164231b803171812b1d0e1b086333a5685d550daf39ecc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Briard, Emmanuelle</creatorcontrib><creatorcontrib>Levillain, Jocelyne</creatorcontrib><creatorcontrib>Ripoll, Jean-Louis</creatorcontrib><title>Access to New Reactive Unsaturated Cycloalkenethiones by Flash Vacuum Thermolysis</title><title>Phosphorus, sulfur, and silicon and the related elements</title><description>The reactive conjugated cycloalkenethiones (3, 4, 5) have been synthesized from the corresponding cycloalkenylsulfanyl compounds under flash vacuum thermolysis (FVT) conditions. The nonconjugated cycloalkenethiones (8, 9) were prepared in the same way, the tautomerisation into cycloalkadienethiols (10, 11) occurred at 77 K. As for the cyclobutenethione 13, only the ring opening products were observed at 77 K.</description><subject>cycloalkenethione</subject><subject>flash vacuum thermolysis</subject><subject>retro-ene</subject><subject>vinylthioketene</subject><issn>1042-6507</issn><issn>1563-5325</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqF0M1Kw0AQB_BFFKzVB_C2LxDdzX6Dl1KsCkVRWq9hstnQaJKV3a01b2-k3op4moGZ3wz8Ebqk5IoSTa4p4bkUxBiiBZdc8yM0oUKyTLBcHI_9OM_GBXWKzmJ8I4SYnJEJep5Z62LEyeNHt8MvDmxqPh1e9xHSNkByFZ4PtvXQvrvepU3jexdxOeBFC3GDX8Futx1ebVzofDvEJp6jkxra6C5-6xStF7er-X22fLp7mM-Wmc2NTJkCbitpjOFaKbBcSSp5zmipCaOKapqXtCKOlkRLxhgIqUUlBKmgZsZZy6aI7u_a4GMMri4-QtNBGApKip9MioNMRqP2pulrHzrY-dBWRYKh9aEO0NsmHqoifaVR3vwr2d-PvwEnF3kb</recordid><startdate>19990101</startdate><enddate>19990101</enddate><creator>Briard, Emmanuelle</creator><creator>Levillain, Jocelyne</creator><creator>Ripoll, Jean-Louis</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990101</creationdate><title>Access to New Reactive Unsaturated Cycloalkenethiones by Flash Vacuum Thermolysis</title><author>Briard, Emmanuelle ; Levillain, Jocelyne ; Ripoll, Jean-Louis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c296t-7a4cd69994877ac476164231b803171812b1d0e1b086333a5685d550daf39ecc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>cycloalkenethione</topic><topic>flash vacuum thermolysis</topic><topic>retro-ene</topic><topic>vinylthioketene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Briard, Emmanuelle</creatorcontrib><creatorcontrib>Levillain, Jocelyne</creatorcontrib><creatorcontrib>Ripoll, Jean-Louis</creatorcontrib><collection>CrossRef</collection><jtitle>Phosphorus, sulfur, and silicon and the related elements</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Briard, Emmanuelle</au><au>Levillain, Jocelyne</au><au>Ripoll, Jean-Louis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Access to New Reactive Unsaturated Cycloalkenethiones by Flash Vacuum Thermolysis</atitle><jtitle>Phosphorus, sulfur, and silicon and the related elements</jtitle><date>1999-01-01</date><risdate>1999</risdate><volume>153</volume><issue>1</issue><spage>387</spage><epage>388</epage><pages>387-388</pages><issn>1042-6507</issn><eissn>1563-5325</eissn><abstract>The reactive conjugated cycloalkenethiones (3, 4, 5) have been synthesized from the corresponding cycloalkenylsulfanyl compounds under flash vacuum thermolysis (FVT) conditions. The nonconjugated cycloalkenethiones (8, 9) were prepared in the same way, the tautomerisation into cycloalkadienethiols (10, 11) occurred at 77 K. As for the cyclobutenethione 13, only the ring opening products were observed at 77 K.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/10426509908546484</doi><tpages>2</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1042-6507 |
ispartof | Phosphorus, sulfur, and silicon and the related elements, 1999-01, Vol.153 (1), p.387-388 |
issn | 1042-6507 1563-5325 |
language | eng |
recordid | cdi_crossref_primary_10_1080_10426509908546484 |
source | Taylor and Francis Science and Technology Collection |
subjects | cycloalkenethione flash vacuum thermolysis retro-ene vinylthioketene |
title | Access to New Reactive Unsaturated Cycloalkenethiones by Flash Vacuum Thermolysis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T17%3A00%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Access%20to%20New%20Reactive%20Unsaturated%20Cycloalkenethiones%20by%20Flash%20Vacuum%20Thermolysis&rft.jtitle=Phosphorus,%20sulfur,%20and%20silicon%20and%20the%20related%20elements&rft.au=Briard,%20Emmanuelle&rft.date=1999-01-01&rft.volume=153&rft.issue=1&rft.spage=387&rft.epage=388&rft.pages=387-388&rft.issn=1042-6507&rft.eissn=1563-5325&rft_id=info:doi/10.1080/10426509908546484&rft_dat=%3Ccrossref_infor%3E10_1080_10426509908546484%3C/crossref_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c296t-7a4cd69994877ac476164231b803171812b1d0e1b086333a5685d550daf39ecc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |